Pilot Study of Bone Mineral Density Changes During Anti-PD-1 Immunotherapy
Recruiting
N/A
Interventional Study
Breast Cancer (Triple Negative Breast Cancer (TNBC))
Renal Cell Carcinoma (Kidney Cancer)
Melanoma (Skin Cancer)
Non-Small Cell Lung Cancer
MSI-H/dMMR Rectal Cancer
Squamous Cell Carcinoma Mouth
Invasive Mammary Carcinoma
Classic Hodgkin Lymphoma
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 25 (estimated)
- Sponsor
- Jessica Mezzanotte Sharpe · Other
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About This Trial
Immune checkpoint inhibitors (ICIs) have revolutionized cancer treatment and work by blocking protein interactions that normally prevent the immune system from recognizing and destroying cancer cells. However, these agents, now approved for over 15 types of cancers and for both early-stage and metastatic disease, are capable of causing inflammation in any organ system of the body that can lead to …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. Age ≥ 18 years.
2. Patients planning to start or within the first four weeks of treatment with anti-PD-1 immune checkpoint inhibitor therapy either alone or in combination with chemotherapy for curative intent for a known cancer diagnosis (use of immunotherapy must be FDA-app…
Contacts